반응 #166887

ord-8cb48817f4f447f590d4c5e920553bb5

반응 방정식

[Cl-].[NH4+]
ammonium chloride
CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
Sodium triacetoxyborohydride
CC(C)(C)OC(=O)NC(CCC=O)(NC(=O)OC(C)(C)C)C(=O)OCc1ccccc1
2,2-bis(tert-butoxycarbonylamino)-5-oxo-pentanoic acid benzyl ester
CCOC(=O)[C@H](C)N.Cl
alanine ethyl ester hydrochloride
CCOC(=O)C(C)NCCCC(NC(=O)OC(C)(C)C)(NC(=O)OC(C)(C)C)C(=O)OCc1ccccc1
2,2-bis(tert-butoxycarbonylamino)-5-(1-ethoxycarbonyl-ethylamino)-pentanoic acid benzyl ester
수율 41.8%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출The aqueous phase was extracted with dichloromethane (2×15 mL)
  2. 2
    건조the combined organic phases were dried over sodium sulfate
  3. 3
    여과filtered
  4. 4
    기타the solvent was removed under reduced pressure
  5. 5
    기타the solvent was removed under reduced pressure

실험 절차

Sodium triacetoxyborohydride (5 g, 23.5 mmol) was added to a solution of 2,2-bis(tert-butoxycarbonylamino)-5-oxo-pentanoic acid benzyl ester (3.34 g, 7.9 mmol) and alanine ethyl ester hydrochloride (3.62 g, 23.5 mmol) in dichloromethane (30 mL). After 1 hour saturated ammonium chloride (10 mL) was added and the mixture was stirred for 5 minutes. The aqueous phase was extracted with dichloromethane (2×15 mL), and the combined organic phases were dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The resulting residue was subjected to flash chromatography with eluent of(10% methanol in ethyl acetate) and hexane. The product-containing fractions were combined and the solvent was removed under reduced pressure to provide 2,2-bis(tert-butoxycarbonylamino)-5-(1-ethoxycarbonyl-ethylamino)-pentanoic acid benzyl ester (1.7 g, 3.3 mmol, 41%). C27H42N2O8 calculated 522.3 observed [M+1]+ 523.3; rt=2.08 min.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08841278B2uspto-grants-2014_09